EP0566348B1 - Zirconiumoxid verbrückte Tone und Glimmer - Google Patents

Zirconiumoxid verbrückte Tone und Glimmer Download PDF

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Publication number
EP0566348B1
EP0566348B1 EP93302835A EP93302835A EP0566348B1 EP 0566348 B1 EP0566348 B1 EP 0566348B1 EP 93302835 A EP93302835 A EP 93302835A EP 93302835 A EP93302835 A EP 93302835A EP 0566348 B1 EP0566348 B1 EP 0566348B1
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Prior art keywords
pillared
clay
zirconia
tsm
pillared clay
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EP93302835A
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French (fr)
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EP0566348A2 (de
EP0566348A3 (de
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Jack Wayne Johnson
John Francis Brody
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ExxonMobil Technology and Engineering Co
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Exxon Research and Engineering Co
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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J29/00—Catalysts comprising molecular sieves
    • B01J29/04—Catalysts comprising molecular sieves having base-exchange properties, e.g. crystalline zeolites
    • B01J29/049—Pillared clays

Definitions

  • This invention relates to a method for preparing zirconia-pillared clays, especially zirconia-pillared fluoromicas.
  • Zirconia-pillared clays are known and are typically prepared by reacting zirconyl chloride with a clay. Such pillared clays are used, for example, in hydrocarbon conversion reactions such as catalytic cracking.
  • US 4248739 describes a method for preparing pillared interlayered clays by reacting smectite clays with high molecular weight cationic metal complexes of metals such as aluminium and zirconium.
  • the metal complexes may be formed by the hydrolysis of the corresponding metal salt, for example zirconium chloride.
  • EP-A-197012 describes pillared interlayered clay molecular sieves where the pillars are made of inorganic oxides inserted into the interlayers of the clay.
  • the precursors of the inorganic oxides are their relative polymeric cationic hydroxy metal complex, i.e. polymerised aluminium chlorohydroxide and/or zirconium chlorohydroxide.
  • the present invention provides a method for producing a zirconia-pillared clay comprising the steps of
  • the process additionally includes step (f) washing the pillared clay product following said calcination step (e) when said clay is a fluoromica.
  • the clays used in the present invention may be any smectite clay or fluoromica, however, the fluoromicas are preferred.
  • zirconyl acetate in the preparation of the clay affords pillared clays with consistently higher crystallinity and significantly higher thermal stability compared with zirconia-pillared clays prepared using other zirconyl compounds such as zirconyl chloride.
  • the zirconia-pillared clays prepared in accordance with the present invention resist collapse when exposed to high temperatures and further maintain a significant surface area when subjected to steam contact.
  • the pillaring solution of the present invention need not be heated, thereby allowing the pillaring reaction to be carried out at ambient temperatures.
  • the catalysts of the present invention are prepared from naturally occurring and synthetic smectites, such as montmorillonite, beidellite, nontronite, saponite, hectorite, and fluorohectorite, and from synthetic fluoromicas such as sodium tetrasilicic mica (NaTSM) and synthetic taeniolite.
  • Smectites and micas are formed of sheets that may be visualized as a sandwich comprising two outer sheets of silicon tetrahedra and an inner layer of aluminum octahedra (i.e. 2:1 layered clay).
  • Clays are generally represented by the general formula: A x [M2 ⁇ 3T4O10(Y)2] where M designates the octahedral cation, T designates the tetrahedral cation, A designates the exchangeable interlayer cations, 0 ⁇ X ⁇ 1, and Y is hydroxy (OH) or fluorine (F) either singly or in combination.
  • the T coordinated ion is commonly Si+4, Al+3, or Fe+3, but could also include several other four-coordinate ions, e.g., P+5, B+3, Ga+3, Cr+3, Ge+4, Be+2, etc.
  • the M coordinated ion is typically Al+3 or Mg+2, but could also include many other possible hexacoordinate ions, e.g., Fe+3, Fe+2, Ni+2, Co+2, Li+, Cr+3, V+2, etc. Mg+2 is preferred in this invention.
  • Synthetic fluoromicas such as sodium tetrasilicic fluoromica (Na[Mg 2.5 Si4O10F2]) and lithium taeniolite (Li[(Mg2Li)Si4O10F2]) undergo swelling in water and other suitable polar solvents. Even though fluoromicas such as these exhibit high layer charge densities, they are capable of undergoing pillaring reactions with large cations. The resulting pillared tetrasilicic micas exhibit good thermal stability and are good catalytic cracking, isomerization, etc., catalysts.
  • the inorganic polymer, or pillaring agent, used to prepare the pillared clays according to the method of the present invention is zirconyl acetate, having a nominal formula of ZrO(OH) 0.5 (CH3COO) 1.5 , which is commercially available.
  • the clay selected is contacted with an aqueous zirconyl acetate solution, which has been diluted with water or another suitable polar solvent, and allowed to react for a time and at a temperature sufficient to form a solid pillared clay material.
  • This contacting is also referred to as pillaring.
  • the reaction will be carried out for about 0.2 to about 24 hours, more preferably, 1 to about 6 hours.
  • the temperature during pillaring ranges between 0 to 50°C, preferably 15 to 35°C. Most preferably the reaction is carried out at room temperature.
  • the amounts of zirconyl acetate solution and clay are chosen such that a desired ratio of Zr/clay will be obtained.
  • the Zr/clay ratio will generally be at least about 4 mmole Zr per g of clay, preferably about 4 to about 46 mmole Zr per g of clay, most preferably about 23 mmoles Zr per g of clay.
  • the resulting solid clay material obtained after contacting may then be separated from solution by filtration or centrifugation followed by washing with distilled water. The washing is preferably continued until the acetic acid odor is not noticeable.
  • the number of washes varies depending on the size of the sample and efficiency of wash. The number of washes is readily determinable by one skilled in the art. Generally about 4-8 washes will be sufficient.
  • the material is then dried between about 50 and 200°C.
  • the material is then calcined at a temperature of about 300°C to 700°C, for about 1 to 24 hours, preferably the material will be held at a temperature at or above about 400°C for about 1 to 24 hours.
  • Calcination decomposes the zirconium hydroxy acetate complex and forms pillars of zirconium oxide.
  • the resulting pillared clays may additionally be washed, for example, with water to remove labilized sodium, formed when utilizing NaTSM, and to obtain enhanced thermal stability.
  • the clays obtained from the present invention are microporous materials typically having two dimensional galleries with 1 to 1.2 nm (10-12 angstrom) height.
  • the surface areas are about 300-400 m2/g and are stable to high temperatures, at or above 700°C.
  • Micropore volumes calculated from the nitrogen isotherm using the t-plot method are typically 0.10 to 0.12 mL/g.
  • the layer repeat distances are 2-2.2 nm (20-22 angstroms) as measured by X-ray diffraction.
  • the zirconia-pillared clays of the present invention exhibit a high degree of order in the interlayer spacing following calcination. After steaming in 100% steam at 760°C for 17 hours, the surface area in some cases is reduced only to about 200 m2/g. Hence, the zirconia-pillared clays of the present invention are capable of acting as catalysts after regeneration in the presence of steam.
  • a series of experiments was carried out to ascertain the affect of the ratio of zirconium to TSM in the pillaring step. All reactions were carried out at room temperature for three hours. A series of eight samples was prepared in which the Zr/TSM ratio was 2.3, 4.6, 9.2, 13.8, 18.4, 23, 34.5, and 46 mmole Zr/g TSM. The amount of zirconyl acetate solution (ZAA), required to obtain the desired Zr/TSM ratio was added to 100 ml of distilled water and stirred at room temperature for 10 minutes. One gram of NaTSM was added and the resulting milky white dispersion was stirred for three hours at room temperature and then separated by centrifugation.
  • ZAA zirconyl acetate solution
  • the solid product was then washed by redispersion in 1 litre of distilled water followed by separation by centrifugation. The washing procedure was repeated until the acetic acid odor was greatly reduced in the decantates (8 washes). The first wash produced a great deal of foam which required about 30 minutes to settle. The foaming disappeared after the second wash. The samples were then filtered and dried at 120°C overnight. X-ray diffraction at this point in the reaction indicated that there was not a high degree of order in the interlayer spacing. Two broad weak peaks at about 2 and 1 nm (20 and 10 angstroms) were present on a high background in the low angle region of the diffraction patterns.
  • the analytical results indicate that at least three-fourths of the sodium in the interlayer space of the NaTSM is exchanged by the polyoxocations. Furthermore, the results show a maximum in zirconium content in the sample prepared with 4.6 mmole Zr/g TSM and a slight decrease in the amount of zirconium incorporated as the amount of zirconyl acetate used in pillaring increases.
  • the surface areas of the zirconia-pillared micas in this series are not as sensitive to the Zr/TSM ratio as are the X-ray crystallinities. As shown in Table I, the surface area of the sample prepared with the lowest amount of zirconyl acetate is only 184 m2/g, but the rest of the samples have surface areas between 290-319 m2/g.
  • the shape of nitrogen uptake isotherms approaches ideal type 1 behavior as the crystallinity of the samples increases.
  • Figure 2 shows the isotherms for three representative samples prepared at Zr/TSM ratios of 2.3, 4.6, and 35 mmole Zr/g TSM.
  • the isotherms for the samples prepared with ratios from 9 to 46 mmole Zr/g TSM were of a shape similar to that of the 35 mmole Zr/g TSM sample shown in the figure.
  • Type 1 isotherms indicate the presence of micropores (R p ⁇ 2 nm (20 ⁇ )) and are characteristic of zeolites and well-ordered pillared clays.
  • the amount of ZAA required to obtain Zr/TSM ratios of 11.6, 23.2, and 34.8 mmole Zr/g TSM was added to 750 ml of distilled water and stirred at room temperature for ten minutes. 10 g of NaTSM was added and the resulting milky white dispersion was stirred for three hours at room temperature.
  • the products were isolated and calcined as described in Example 1. Half of each of the products was then stirred with 700 ml of distilled water at room temperature for 3 hours and then separated by centrifugation. This procedure was repeated three times over a twenty four hour period. The samples were filtered and dried at 120°C overnight. The samples were then calcined in air at 250°C for two hours then heated to 400°C for two hours.
  • the ZrTSM samples were spread in a shallow layer inside quartz tubes and inserted into a steaming apparatus designed for deactivating cracking catalysts. The samples were exposed to pure steam flowing at approximately 1200 to 1400 cm3/min for 17 hours at controlled temperature.
  • TABLE III Surface Area (m2/g) of ZrTSM After Steaming 17 Hours in 100% Steam mmole Zr/g TSM Unsteamed 650°C Steam 700°C Steam 760°C Steam 11.6, unwashed 308 217 173 95 11.6, washed 332 254 218 172 23.2, unwashed 328 283 241 20 23.2, washed 339 306 260 194 34.8, unwashed 311 278 234 20 34.8, washed 339 298 258 184
  • the washed sample of zirconia-pillared tetrasilicic mica after 760°C steaming had a surface area of 194 m2/g and a micropore volume of 0.073 ml/g, though the layer spacing line is no longer detectable in the X-ray powder diffraction pattern.
  • a sample of zirconia-pillared mica was prepared by treating a dilute aqueous suspension of size-fractionated NaTSM with an aqueous solution of zirconyl chloride, the pillaring agent commonly employed by the prior art, followed by washing and calcination at 400°C to form zirconia pillared TSM.
  • the sample was prepared using a solution of ZrOCl2 ⁇ 4H2O that had been refluxed for 24 hours prior to pillaring at room temperature.
  • the layer spacing of the sample was 2.1 nm (21 angstroms), however the sample did not show a high degree of order as demonstrated by its X-ray powder diffraction pattern.
  • the peak representing the layer spacing was only a shoulder on the low angle background unlike the sharp peak observed for NaTSM pillared with zirconyl acetate in accordance with the present invention.
  • the sample exhibited a surface area of only 231 m2/g. Additionally, reproducible results were not obtainable.
  • the 2.1 nm (21 angstrom) shoulder observed previously in the X-ray powder diffraction pattern was absent after calcination of the product at 400°C and the surface area was only 108 m2/g.
  • Example 6 Zirconia-pillared clay using montmorillonite
  • a commercially available montmorillonite (bentonite HPM-20 from American Colloid Company) was pillared with zirconia following a procedure similar to that of Example 1.
  • ZAA solution 100 mL, 232 mmole Zr
  • 10.0 g montmorillonite was added and the resulting suspension was stirred at ambient temperature for 3 hours.
  • the solid was separated by filtration and dried at 120°C.
  • the sample was then calcined in a muffle furnace at 200°C for two hours, heated to 400°C at 50°C/hour, and held at 400°C for 2 hours.
  • the layer spacing measured by X-ray diffraction was 2.02 nm (20.2 ⁇ ) and the surface area was 388 m2/g. Steaming tests were carried out on this sample of Zr-montmorillonite as described in Example 3. After steam treatment at 650°C for 17 hours, the surface area is 228 m2/g; after steam treatment at 700°C for 17 hours, the surface area is 86 m2/g; and steam treatment at 750°C for 17 hours, the surface area is 20 m2/g.
  • X-ray diffraction patterns of the sample before and after steam treatments are displayed in Figure 1, View D. The diffraction line corresponding to the ⁇ 2 nm ( ⁇ 20 ⁇ ) layer spacing is maintained after 650°C steaming, but disappears after steam treatment at 700 or 760°C, in conjunction with loss of most of the surface area.
  • Example 7 An olefin isomerization reaction catalyzed by zirconia-pillared tetrasilicic mica
  • Zirconia-pillared tetrasilicic mica (Zr-TSM) was prepared according to the procedure of Example 2 using 23 mmole Zr/g clay. Part of the sample was washed after calcination and recalcined.
  • alumina-pillared tetrasilicic mica was prepared in a similar manner using aluminum chlorhydrol solution in place of the ZAA solution. The samples were characterized by measuring their layer repeat distance by X-ray diffraction and their surface areas by nitrogen adsorption. The results are given in Table V. The results for a standard c-Al2O3 catalyst that had been impregnated with 0.9% Cl have also been included for comparison.
  • the solid acidity of the pillared clays was assessed by measuring the rate of isomerization of a model olefin, 2-methylpent-2-ene (2MP2), in the vapor phase over the pillared clay catalysts.
  • the reactions were carried out in a standard fixed bed reactor equipped with a furnace for temperature control, flow controllers and saturators to control the feed stream, and an online gas chromatograph to identify the products of the reaction. Pillared clay samples (1 g) were pretreated at 500°C in 500 cc/min H2 flow, and then purged with 500 cc/min He while cooling to 250°C. 2MP2 (7% in He) was flowed over the catalyst at atmospheric pressure for one hour at 250°C, then the temperature was raised to 350°C. The conversions and product ratios measured at 350°C and 2 hour total time on stream are reported in Table V.
  • the results of the 2MP2 isomerization tests show that the postcalcination wash enhances the acidity of the pillared micas.
  • the sample of Zr-TSM that was not washed showed a 2MP2 conversion of 38.6% while the Zr-TSM after washing and recalcination gave a 2MP2 conversion of 65.2%.
  • the distribution of the strengths of the acid sites in the solid is addressed by the rate ratios in Table V.
  • the isomerization of 2MP2 to 4-methylpent-2-ene (4MP2) requires only a hydrogen shift and can be catalyzed by a relatively weak acid site.
  • the isomerization of 2MP2 to 3-methylpent-2-ene (3MP2) involves a methyl shift and requires a moderately strong acid site.
  • the isomerization of 2MP2 to 2,3-dimethylbutene (23DMB) is a more extensive skeletal rearrangement and requires a strong acid site to facilitate it.
  • the ratio of 3MP2/2MP2 shown in the results for the washed Zr-TSM shows a relatively large proportion of the acid sites in this material have a moderate level of acidity, while the low ratio 23DMB/2MP2 show that there are few acid sites of high strength.
  • the acidity distribution in Zr-TSM is similar to that found in Al-TSM, and narrower than that found in Cl/Al2O3 because there are relatively fewer strong acid sites.

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  • Chemical & Material Sciences (AREA)
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  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
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  • Silicates, Zeolites, And Molecular Sieves (AREA)
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Claims (10)

  1. Verfahren zur Herstellung eines Tons mit Zwischenlagen aus Zirconiumdioxid, bei dem
    (a) ein Ton ausgewählt aus smektischen Tonen und Fluorglimmern mit einer Lösung von Zirconylacetat gemischt wird, um ein Tonprodukt mit Zwischenlagen zu bilden,
    (b) das Tonprodukt mit Zwischenlagen aus der Lösung abgetrennt wird,
    (c) das abgetrennte Tonprodukt mit Zwischenlagen mit Wasser gewaschen wird,
    (d) das abgetrennte, gewaschene Tonprodukt mit Zwischenlagen bei einer Temperatur von etwa 50 bis 200°C getrocknet wird,
    (e) das getrocknete Tonprodukt mit Zwischenlagen bei einer Temperatur von etwa 300 bis 700°C calciniert wird.
  2. Verfahren nach Anspruch 1, bei dem der Ton Fluorglimmer ist.
  3. Verfahren nach Anspruch 2, bei dem der Fluorglimmer Tetrakieselsäure-Glimmer ist.
  4. Verfahren nach Anspruch 2 oder 3, bei dem außerdem das Tonprodukt mit Zwischenlagen nach der Calcinierungsstufe (e) gewaschen wird.
  5. Verfahren nach einem der vorhergehenden Ansprüche, bei dem die Mengen an Ton und an Zirconylacetatlösung so gewählt werden, daß das erhaltene Verhältnis von Zirconium zu Ton mindestens etwa 4 mmol Zirconiumdioxid pro gramm Ton beträgt.
  6. Verfahren nach einem der vorhergehenden Ansprüche, bei dem die Mischstufe (a) etwa 0,2 bis etwa 24 Stunden lang durchgeführt wird.
  7. Verfahren nach einem der vorhergehenden Ansprüche, bei dem die Mischstufe (a) bei einer Temperatur zwischen 0 und 50°C, vorzugsweise 15 bis 35°C durchgeführt wird.
  8. Verfahren nach einem der vorhergehenden Ansprüche, bei dem das getrocknete Tonprodukt mit Zwischenlagen während der Calcinierungsstufe (e) bei oder oberhalb von 400°C mindestens etwa 1 bis etwa 24 Stunden lang calciniert wird.
  9. Verfahren nach einem der vorhergehenden Ansprüche, bei dem der resultierende Ton mit Zwischenlagen aus Zirconiumdioxid einen Schichtwiederholungsabstand von etwa 2 bis 2,2 nm (20 bis 22 Å) aufweist.
  10. Verfahren nach einem der vorhergehenden Ansprüche, bei dem der resultierende Ton mit Zwischenlagen aus Zirconiumdioxid Ganghöhen von 1 bis 1,2 nm (10 bis 12 Å) hat.
EP93302835A 1992-04-13 1993-04-13 Zirconiumoxid verbrückte Tone und Glimmer Expired - Lifetime EP0566348B1 (de)

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US07/867,581 US5248644A (en) 1992-04-13 1992-04-13 Zirconia-pillared clays and micas

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EP0566348A3 EP0566348A3 (de) 1993-11-03
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US6669743B2 (en) 1997-02-07 2003-12-30 Exxonmobil Research And Engineering Company Synthetic jet fuel and process for its production (law724)
US6822131B1 (en) 1995-10-17 2004-11-23 Exxonmobil Reasearch And Engineering Company Synthetic diesel fuel and process for its production

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US5733439A (en) * 1994-03-18 1998-03-31 Uop Hydrocarbon conversion processes using substituted fluoride smectite clays
FR2720387B1 (fr) * 1994-05-30 1996-07-26 Inst Francais Du Petrole Argile synthétisée en milieu fluoré et acide puis montée par un procédé de pontage particulier.
US6296757B1 (en) 1995-10-17 2001-10-02 Exxon Research And Engineering Company Synthetic diesel fuel and process for its production
FR2745203B1 (fr) * 1996-02-27 1998-04-10 Inst Francais Du Petrole Catalyseur comprenant un phyllosilicate 2:1 dioctaedrique prepare en milieu fluorure et procede d'hydroconversion de charges petrolieres
FR2745728B1 (fr) * 1996-03-08 1998-04-10 Inst Francais Du Petrole Catalyseur comprenant un phyllosilicate 2:1 trioctaedrique prepare en milieu fluorure et procede d'hydroconversion de charges petrolieres
JP2000514029A (ja) * 1996-06-11 2000-10-24 エクソン リサーチ アンド エンジニアリング カンパニー 安定な架橋粘土及び、蝋質供給原料の水素転化用触媒としてのその使用
AU8659098A (en) * 1997-07-15 1999-02-10 Allied-Signal Inc. Chemically modified micas for removal of cesium salts from aqueous solution
DE102007025442B4 (de) * 2007-05-31 2023-03-02 Clariant International Ltd. Verwendung einer Vorrichtung zur Herstellung eines Schalenkatalysators und Schalenkatalysator
DE102007025223A1 (de) 2007-05-31 2008-12-04 Süd-Chemie AG Zirkoniumoxid-dotierter VAM-Schalenkatalysator, Verfahren zu dessen Herstellung sowie dessen Verwendung
DE102007025444A1 (de) * 2007-05-31 2008-12-11 Süd-Chemie AG VAM-Schalenkatalysator, Verfahren zu dessen Herstellung sowie dessen Verwendung
DE202008017277U1 (de) * 2008-11-30 2009-04-30 Süd-Chemie AG Katalysatorträger
US10004957B2 (en) 2015-02-19 2018-06-26 Acushnet Company Weighted iron set
US10357697B2 (en) 2015-02-19 2019-07-23 Acushnet Company Weighted iron set
US9750993B2 (en) 2015-02-19 2017-09-05 Acushnet Company Weighted iron set
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Cited By (2)

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Publication number Priority date Publication date Assignee Title
US6822131B1 (en) 1995-10-17 2004-11-23 Exxonmobil Reasearch And Engineering Company Synthetic diesel fuel and process for its production
US6669743B2 (en) 1997-02-07 2003-12-30 Exxonmobil Research And Engineering Company Synthetic jet fuel and process for its production (law724)

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JPH0648724A (ja) 1994-02-22
CA2092464A1 (en) 1993-10-14
CA2092464C (en) 2001-12-04
DE69301330D1 (de) 1996-02-29
DE69301330T2 (de) 1996-06-27
US5248644A (en) 1993-09-28
EP0566348A2 (de) 1993-10-20
EP0566348A3 (de) 1993-11-03

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